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Glp Jobs (NOW HIRING)

Frontage Laboratories

QA Specialist-GLP/BIO

Exton, PA · On-site

Director BIO GLP Quality assurance Full-time Position/Job Summary: Are you ready for a role that will combine your thirst for scientific knowledge and eye for quality. Then you are the perfect fit ...

Labcorp

Lead Internal Auditor, GLP/GCP

Indianapolis, IN · On-site

Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN ! Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Lead Internal Auditor plays a pivotal ...

Labcorp

Lead Internal Auditor, GLP/GCP

Indianapolis, IN · On-site

Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN ! Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Lead Internal Auditor plays a pivotal ...

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How much do glp jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for glp in the United States is $22.90, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals working in GLP (Good Laboratory Practice) roles, and how can they be addressed?

Professionals in GLP roles often encounter challenges such as maintaining meticulous documentation, ensuring strict protocol adherence, and staying updated with evolving regulatory standards. These responsibilities require strong attention to detail and effective time management. Collaboration with cross-functional teams, such as quality assurance and laboratory staff, is essential to ensure compliance and data integrity. Regular training and open communication channels can help address these challenges and support a smooth workflow.

What is the difference between Glp vs Pharmacist?

AspectGlpPharmacist
Required CredentialsCertification in Good Laboratory Practice (GLP) standardsDoctor of Pharmacy (PharmD) or equivalent, licensure
Work EnvironmentLaboratories, research facilitiesPharmacies, hospitals, clinics
Industry UsageRegulatory compliance, research oversightMedication dispensing, patient care
Common Search/ComparisonGLP vs PharmacistPharmacist roles, responsibilities

GLP professionals focus on ensuring laboratory compliance with regulatory standards in research settings, while pharmacists are healthcare providers responsible for dispensing medications and advising patients. Both roles require specialized knowledge but serve different functions within the healthcare and research industries.

What is a GLP (Good Laboratory Practice) professional?

GLP professionals are individuals who ensure that laboratory studies are conducted in accordance with Good Laboratory Practice regulations. These standards are designed to ensure the quality, reliability, and integrity of non-clinical laboratory studies, particularly those related to the safety of pharmaceuticals, chemicals, and other products. GLP professionals may work in various roles, such as quality assurance, study direction, data management, or laboratory operations. Their responsibilities include maintaining documentation, overseeing compliance, and supporting audits or inspections. By adhering to GLP guidelines, they help ensure that data generated in the lab are credible and accepted by regulatory agencies.

What are the key skills and qualifications needed to thrive as a GLP (Good Laboratory Practice) specialist, and why are they important?

To thrive as a GLP Specialist, you need a solid background in laboratory sciences, quality assurance, and regulatory compliance, often supported by a relevant degree and experience in GLP environments. Familiarity with laboratory information management systems (LIMS), audit processes, and documentation standards is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure data integrity, regulatory compliance, and the smooth operation of laboratory processes subject to strict guidelines.
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Glp jobs near you
Infographic showing various Glp job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 4% Part Time, 1% Temporary, 10% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $47,622 per year, or $22.9 per hour.

GLP Study Director - In Vivo Services

Pacific BioLabs

Hercules, CA

$120K - $150K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 19 days ago

Job description

Description

Pacific BioLabs is an independent CRO providing cGMP/GLP testing in toxicology, biocompatibility, pharmacology, analytical chemistry, and microbiology. We are currently hiring to support our clients in the pharmaceutical, biotech, and medical device fields. Join us in our mission to improve public health through science! 


PBL has immediate openings for full time GLP Study Director in the In Vivo Services Department. As the single point of study management and control, GLP Study Director will be responsible for the overall conduct of GLP studies focused on medical devices and pharmaceutical products ensuring compliance with GLP regulations.


Responsibilities of the GLP Study Director include:

  • Serve as the Study Director for a variety of biocompatibility, safety, and efficacy studies for medical devices and pharmaceutical products in accordance with Good Laboratory Practice (GLP) for Nonclinical Laboratory Studies (Title 21, Part 58).
  • Overall responsibility for the technical conduct of GLP studies that includes study design, protocol assembly, study amendment management, oversight of testing personnel, study execution, data interpretation and analysis, and reporting.
  • Working proactively with Sponsors in developing protocols that follow PBL SOPs, GLPs, ISO, etc. and other applicable regulatory guidelines. Ensuring that any protocol changes are approved and documented in accordance with GLP practices.
  • Working collaboratively with department management, veterinarian personnel, and Quality Assurance in exceeding Sponsor expectations in the conduct of studies.
  • Serve as Multistudy Project Coordinator.
  • Ability to review study data in all phases of study execution and direct oversight of completion of corrective actions, deviations, and CAPA generation and review.
  • Ensure that unanticipated responses of study data are corrected, accurately recorded, verified, and documentation corrective actions are taken in accordance with regulatory guidelines.
  • Oversee and manage subcontracted GLP testing with approved vendors and qualified Principal Investigator personnel.
  • QC review of raw data for technical content and regulatory compliance.
  • Managing applicable study deviation investigations.
  • Collaboration with Business Development on Sponsor outreach and testing quotes.
  • Maintaining a safe and orderly laboratory and ensuring compliance with all safety policies and practices.

Requirements

  • Bachelor's Degree (B.S./B.A.) or equivalent in a scientifically related discipline. Related Master's Degree (M.S./M.A.) or Ph.D. preferred. Applicants with AALAS certification highly desired.
  • Prefer a minimum of 5-6 years of related experience. Applicants with CRO experience highly desired.
  • Broad understanding of GLP policies and regulatory requirements (FDA, CDC, USDA) highly desired. 
  • A combination of related experience and knowledge may substitute for education and experience.
  • Must have demonstrated knowledge of laboratory animal science, toxicology, and histology.
  • Ability to handle multiple projects of varying complexity and duration, prioritize work, and meet Sponsor deadlines.
  • Exhibits strong technical skills and the ability to critically evaluate raw data and results with minimal supervision.
  • Excellent written, reporting, and verbal communication skills and attention to detail.
  • Must be able to sit and/or stand for extended periods of time.
  • Must be able to work with persons of diverse background.
  • Proficient in using Microsoft Office including Word, Excel, and Power Point.
  • Must be highly motivated and capable of working independently or under minimum supervision to deliver results under tight deadlines.
  • Able to lift 10 - 25 pounds.

The pay range for this position is $120,000 to $150,000 per year. The base pay offered will take into account internal equity and also may vary depending on the candidate's job-related knowledge, skills, and experience among other factors. This position will be eligible for medical, dental, vision, life insurance, 401k, and other benefits.


PBL is an equal opportunity employer committed to diversity and inclusion. PBL considers all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veterans' status, or any other legally protected factors.

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